Objective and independent

We are an independent and autonomous service provider and look forward to supporting your company. Our core competence lies in the area of product development, with special emphasis on regulatory affairs for human and veterinary medicinal products. Since its establishment YES has extended its activities to all the EU member states and in 2009 to countries in other regions (Emerging Markets).

Rapid and reliable

You want to minimize your time to market – we ensure regulatory compliance. We also provide support in connection with the resource-efficient development and safeguarding of your products during their lifecycle.

Throughout the entire lifecycle

We have the right team: YES employs more than 100 specialists in the fields of biology, chemistry, food chemistry, medicine, nutritional science, pharmacology/toxicology, veterinary medicine and engineering. We provide continuous support throughout the entire lifecycle of your medicinal products and medical devices.

Your experienced partners

• We work for more than 250 customers in Germany and abroad and are in constant contact with the regulatory authorities in connection with a diverse range of projects.
•  We are well acquainted with different corporate cultures, variations in data quality, specialist areas and opportunities – and with the current requirements.
• We integrate the current regulatory, scientific and technical requirements into your product development and maintenance activities.
• We take account of the currently applicable national requirements and interpretations. For this purpose we have a subsidiary in Austria, a bureau de liaison in France, plus partner companies in all the EU member states and contacts in other regions.